scholarly article | Q13442814 |
P50 | author | Alpha Yap | Q37377160 |
Nicole Den Elzen | Q55298817 | ||
P2093 | author name string | Gang Ren | |
Madhavi P Maddugoda | |||
Carmen V Buttery | |||
P2860 | cites work | AMER1 regulates the distribution of the tumor suppressor APC between microtubules and the plasma membrane | Q24297032 |
Mammalian Pins is a conformational switch that links NuMA to heterotrimeric G proteins | Q24313402 | ||
APC and EB1 function together in mitosis to regulate spindle dynamics and chromosome alignment | Q24536199 | ||
Actin-dependent membrane association of the APC tumour suppressor in polarized mammalian epithelial cells | Q28363074 | ||
Direct cadherin-activated cell signaling: a view from the plasma membrane | Q28756060 | ||
Experimental and theoretical study of mitotic spindle orientation | Q29396188 | ||
Morphogenetic roles of classic cadherins | Q29614941 | ||
Asymmetric cell divisions promote stratification and differentiation of mammalian skin | Q29620393 | ||
Depletion of E-cadherin disrupts establishment but not maintenance of cell junctions in Madin-Darby canine kidney epithelial cells | Q30442081 | ||
Ena/VASP proteins can regulate distinct modes of actin organization at cadherin-adhesive contacts | Q30476860 | ||
Mammalian spindle orientation and position respond to changes in cell shape in a dynein-dependent fashion | Q30477500 | ||
Integrin-mediated adhesion orients the spindle parallel to the substratum in an EB1- and myosin X-dependent manner | Q30479119 | ||
Cadherins in embryonic and neural morphogenesis | Q33938474 | ||
Cadherin-directed actin assembly: E-cadherin physically associates with the Arp2/3 complex to direct actin assembly in nascent adhesive contacts | Q34117282 | ||
Asymmetric cell division: fly neuroblast meets worm zygote | Q34132774 | ||
Asymmetric cell division. | Q34326914 | ||
Adhesion signaling: how beta-catenin interacts with its partners | Q34395476 | ||
Dynein at the cortex | Q34495155 | ||
Asymmetric cell division: microtubule dynamics and spindle asymmetry. | Q34634844 | ||
Control of cell polarity and mitotic spindle positioning in animal cells | Q35041105 | ||
Dare to be different: asymmetric cell division in Drosophila, C. elegans and vertebrates | Q35868625 | ||
Orientation of spindle axis and distribution of plasma membrane proteins during cell division in polarized MDCKII cells | Q36534977 | ||
Cell shape and cell division | Q36625784 | ||
Cell regulation by the Apc protein Apc as master regulator of epithelia. | Q37116480 | ||
The immunoglobulin-like cell adhesion molecule nectin and its associated protein afadin. | Q37204309 | ||
Planar spindle orientation and asymmetric cytokinesis in the mouse small intestine | Q38317735 | ||
Morphogenesis of the polarized epithelial cell phenotype | Q38684855 | ||
A dileucine motif targets E-cadherin to the basolateral cell surface in Madin-Darby canine kidney and LLC-PK1 epithelial cells. | Q40811578 | ||
Differential regulation of endogenous cadherin expression in Madin-Darby canine kidney cells by cell-cell adhesion and activation of beta -catenin signaling | Q40889576 | ||
The role of DE-cadherin during cellularization, germ layer formation and early neurogenesis in the Drosophila embryo | Q42462757 | ||
Adherens junctions inhibit asymmetric division in the Drosophila epithelium | Q42499987 | ||
Drosophila E-cadherin regulates the orientation of asymmetric cell division in the sensory organ lineage | Q42516585 | ||
Dynein binds to beta-catenin and may tether microtubules at adherens junctions. | Q43754950 | ||
E-cadherin homophilic ligation directly signals through Rac and phosphatidylinositol 3-kinase to regulate adhesive contacts | Q43823908 | ||
Echinoid is a component of adherens junctions that cooperates with DE-Cadherin to mediate cell adhesion | Q47070048 | ||
The orientation of cell divisions determines the shape of Drosophila organs. | Q47070632 | ||
Testing hypotheses for the functions of APC family proteins using null and truncation alleles in Drosophila | Q47072837 | ||
Orientation of asymmetric stem cell division by the APC tumor suppressor and centrosome. | Q52100403 | ||
Dynein and dynactin are localized to astral microtubules and at cortical sites in mitotic epithelial cells. | Q52187841 | ||
Drosophila APC2 and Armadillo participate in tethering mitotic spindles to cortical actin. | Q52591547 | ||
Spindle misorientation in tumors from APC(min/+) mice. | Q53314237 | ||
The extracellular matrix guides the orientation of the cell division axis. | Q53656268 | ||
Cytokinesis in animal cells | Q68760577 | ||
P433 | issue | 16 | |
P304 | page(s) | 3740-3750 | |
P577 | publication date | 2009-06-24 | |
P1433 | published in | Molecular Biology of the Cell | Q2338259 |
P1476 | title | Cadherin adhesion receptors orient the mitotic spindle during symmetric cell division in mammalian epithelia | |
P478 | volume | 20 |
Q89108028 | Aberrant endocytosis leads to the loss of normal mitotic spindle orientation during epithelial glandular morphogenesis |
Q60301609 | Actomyosin-Driven Tension at Compartmental Boundaries Orients Cell Division Independently of Cell Geometry In Vivo |
Q38016773 | Adherens junctions and stem cells. |
Q34122302 | Adherens junctions: from molecules to morphogenesis |
Q35818227 | An aberrant nuclear localization of E-cadherin is a potent inhibitor of Wnt/β-catenin-elicited promotion of the cancer stem cell phenotype |
Q58067537 | Analysis of a vinculin homolog in a sponge (phylum Porifera) reveals that vertebrate-like cell adhesions emerged early in animal evolution |
Q33769261 | Cadherins and Pak1 control contact inhibition of proliferation by Pak1-betaPIX-GIT complex-dependent regulation of cell-matrix signaling. |
Q34168468 | Cell adhesion in regulation of asymmetric stem cell division |
Q38677606 | Cell adhesion molecule control of planar spindle orientation. |
Q26858973 | Cell division and the maintenance of epithelial order |
Q37562683 | Cell division orientation is coupled to cell-cell adhesion by the E-cadherin/LGN complex |
Q35679252 | Cell shape impacts on the positioning of the mitotic spindle with respect to the substratum. |
Q42514755 | Cell-cell adhesion accounts for the different orientation of columnar and hepatocytic cell divisions. |
Q38248934 | Centrosome positioning in polarized cells: common themes and variations. |
Q36497518 | Centrosome positioning in vertebrate development |
Q26785528 | Connections between cadherin-catenin proteins, spindle misorientation, and cancer |
Q35041609 | Distinct roles of cadherin-6 and E-cadherin in tubulogenesis and lumen formation |
Q41148057 | E-cadherin and LGN align epithelial cell divisions with tissue tension independently of cell shape |
Q33687283 | E-cadherin is required for centrosome and spindle orientation in Drosophila male germline stem cells |
Q27313451 | Effect of Cell Shape and Dimensionality on Spindle Orientation and Mitotic Timing |
Q91942694 | Eph signaling controls mitotic spindle orientation and cell proliferation in neuroepithelial cells |
Q30495669 | Epicardial spindle orientation controls cell entry into the myocardium |
Q37968480 | Epithelial cell polarity, stem cells and cancer |
Q26825041 | Epithelial polarity--generating and integrating signals from the ECM with integrins |
Q64243670 | Evolution as a guide for experimental cell biology |
Q50627126 | FAK transduces extracellular forces that orient the mitotic spindle and control tissue morphogenesis. |
Q27009493 | Force and the spindle: mechanical cues in mitotic spindle orientation |
Q37725724 | Hereditary diffuse gastric cancer: translation of CDH1 germline mutations into clinical practice. |
Q30427386 | Integrins and cadherins join forces to form adhesive networks |
Q27313566 | Interphase adhesion geometry is transmitted to an internal regulator for spindle orientation via caveolin-1. |
Q36030193 | JAM-A regulates cortical dynein localization through Cdc42 to control planar spindle orientation during mitosis. |
Q30434467 | LGN regulates mitotic spindle orientation during epithelial morphogenesis |
Q38015243 | Let's huddle to prevent a muddle: centrosome declustering as an attractive anticancer strategy |
Q47132771 | Loss of E-cadherin provides tolerance to centrosome amplification in epithelial cancer cells. |
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Q39571912 | Matrix stiffening sensitizes epithelial cells to EGF and enables the loss of contact inhibition of proliferation |
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Q36417737 | Mitotic cells contract actomyosin cortex and generate pressure to round against or escape epithelial confinement |
Q36191191 | Myosin II isoforms identify distinct functional modules that support integrity of the epithelial zonula adherens |
Q30513859 | Myosin-X functions in polarized epithelial cells |
Q27004163 | Myosins in cell junctions |
Q42428878 | PAR-6, but not E-cadherin and β-integrin, is necessary for epithelial polarization in C. elegans |
Q37267940 | Par1b links lumen polarity with LGN-NuMA positioning for distinct epithelial cell division phenotypes. |
Q36823704 | Parkin deficiency contributes to pancreatic tumorigenesis by inducing spindle multipolarity and misorientation. |
Q38160892 | Patterns in space: coordinating adhesion and actomyosin contractility at E-cadherin junctions. |
Q38107433 | Random chromosome segregation in mouse intestinal epithelial stem cells. |
Q62485079 | Role of adherens junctions and apical-basal polarity of neural stem/progenitor cells in the pathogenesis of neurodevelopmental disorders: a novel perspective on congenital Zika syndrome |
Q27315980 | Scribble modulates the MAPK/Fra1 pathway to disrupt luminal and ductal integrity and suppress tumour formation in the mammary gland |
Q36784413 | Single-Cell Lineage Tracing Reveals that Oriented Cell Division Contributes to Trabecular Morphogenesis and Regional Specification |
Q35903531 | Spindle position in symmetric cell divisions during epiboly is controlled by opposing and dynamic apicobasal forces |
Q52641939 | Structural centrosome aberrations promote non-cell-autonomous invasiveness. |
Q39409518 | Suppression of Rac1 activity at the apical membrane of MDCK cells is essential for cyst structure maintenance. |
Q42464662 | Symmetrical and asymmetrical division analysis provides evidence for a hierarchy of prostate epithelial cell lineages |
Q39242330 | Symmetry Does not Come for Free: Cellular Mechanisms to Achieve a Symmetric Cell Division. |
Q34692456 | Syntaxin 16 regulates lumen formation during epithelial morphogenesis. |
Q28255263 | The APC tumor suppressor is required for epithelial cell polarization and three-dimensional morphogenesis |
Q34345692 | The LKB1 tumor suppressor controls spindle orientation and localization of activated AMPK in mitotic epithelial cells |
Q39242277 | The Midbody and its Remnant in Cell Polarization and Asymmetric Cell Division |
Q38869306 | The ins(ide) and outs(ide) of asymmetric stem cell division |
Q58740977 | The last-born daughter cell contributes to division orientation of Drosophila larval neuroblasts |
Q37405061 | The p38-interacting protein (p38IP) regulates G2/M progression by promoting α-tubulin acetylation via inhibiting ubiquitination-induced degradation of the acetyltransferase GCN5. |
Q39000953 | The special case of hepatocytes: unique tissue architecture calls for a distinct mode of cell division |
Q35057143 | Thiazolidinediones inhibit MDCK cyst growth through disrupting oriented cell division and apicobasal polarity |
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Q37583348 | Type VII collagen regulates expression of OATP1B3, promotes front-to-rear polarity and increases structural organisation in 3D spheroid cultures of RDEB tumour keratinocytes. |
Q38734544 | ZO-1 interactions with F-actin and occludin direct epithelial polarization and single lumen specification in 3D culture. |
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